Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894469
rs104894469
PAX9 ; LOC105370455
2 0.925 0.080 14 36663043 missense variant G/A;T snv 4.0E-06 0.800 1.000 1 2003 2003
dbSNP: rs1555316697
rs1555316697
PAX9 ; LOC105370455
2 1.000 0.080 14 36662951 missense variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs104894467
rs104894467
PAX9 ; LOC105370455
1 1.000 0.080 14 36663232 stop gained A/C;T snv 8.0E-06 0.700 0
dbSNP: rs1131692057
rs1131692057
PAX9 ; LOC105370455
2 0.925 0.080 14 36662092 start lost G/A snv 0.700 0
dbSNP: rs121917720
rs121917720
PAX9 ; LOC105370455
1 1.000 0.080 14 36663031 missense variant C/T snv 0.700 0
dbSNP: rs28933970
rs28933970
PAX9 ; LOC105370455
2 0.925 0.080 14 36662954 missense variant T/C snv 0.700 0
dbSNP: rs28933971
rs28933971
PAX9 ; LOC105370455
3 0.882 0.080 14 36662975 missense variant G/A;C snv 0.700 0
dbSNP: rs28933972
rs28933972
PAX9 ; LOC105370455
1 1.000 0.080 14 36662968 missense variant C/T snv 0.700 0
dbSNP: rs587776350
rs587776350
PAX9 ; LOC105370455
1 1.000 0.080 14 36663228 missense variant C/G snv 0.700 0